Canonical Allele Identifier: CA2326525338
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18785709G= , CM000681.2:g.18785709G= GRCh38
NC_000019.9:g.18896519G= , CM000681.1:g.18896519G= GRCh37
NC_000019.8:g.18757519G= NCBI36
NG_007070.1:g.10596C=

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1632C= MANE Select ENSP00000222271.2:p.Asp544=
ENST00000222271.6:c.1632C= ENSP00000222271.2:p.Asp544=
ENST00000425807.1:c.1473C= ENSP00000403792.1:p.Asp491=
ENST00000542601.6:c.1533C= ENSP00000439156.2:p.Asp511=
NM_000095.2:c.1632C= NP_000086.2:p.Asp544=
NM_000095.3:c.1632C= MANE Select NP_000086.2:p.Asp544=